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NCT06155357 | WITHDRAWN | Atrial Fibrillation

A Study of a Lifestyle Program on Recurrent Atrial Fibrillation
Sponsor:

Mayo Clinic

Information provided by (Responsible Party):

Amanda R. Banikowsk

Brief Summary:

The purpose of this study is to examine the impact of a comprehensive lifestyle intervention, including cardiac rehabilitation, prior to catheter ablation (a procedure to stop abnormal electrical signals in the heart), on Atrial Fibrillation (AF)-related symptoms.

Condition or disease

Atrial Fibrillation

Intervention/treatment

Multicomponent lifestyle intervention program

Phase

NA

Study Type : INTERVENTIONAL
Estimated Enrollment : 0 participants
Masking : NONE
Primary Purpose : HEALTH_SERVICES_RESEARCH
Official Title : Pre-habilitation Multicomponent Lifestyle Program for Patients Undergoing Ablation for Atrial Fibrillation
Actual Study Start Date : 2024-09
Estimated Primary Completion Date : 2025-08
Estimated Study Completion Date : 2026-08

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Paroxysmal or persistent atrial fibrillation.
  • * Planned elective catheter ablation of AF.
Exclusion Criteria
  • * Prior catheter ablation.
  • * Presence of pacemaker/ICD.
  • * Longstanding persistent AF.
  • * Uncontrolled AF (including poor rate control or tachycardia-mediated cardiomyopathy requiring urgent cardioversion/ablation at the clinician's assessment).
A Study of a Lifestyle Program on Recurrent Atrial Fibrillation

Location Details

NCT06155357

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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

Not yet recruiting

United States, Minnesota

Mayo Clinic in Rochester

Rochester, Minnesota, United States, 55905